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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of metamorphic geology 9 (1991), S. 0 
    ISSN: 1525-1314
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1525-1314
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: The microstructures in the Erro-Tobbio peridotite indicate several stages of recrystallization of olivine + titanian clinohumite-bearing assemblages. The development of these assemblages is closely associated with serpentinite mylonites, in which they occur in shear bands and foliations and are inferred to have grown synkinematically, in veins, and as post-kinematic radial aggregates. In the peridotite wall-rock adjacent to these mylonites, the same assemblages have recrystallized statically at the expense of original olivine and pyroxenes, mesh-textured chrysolite and antigorite veins. In addition, the olivine-bearing assemblage occurs in widespread vein systems. The brittle deformation of the peridotite resulting in the development of these vein systems is closely related to ductile deformation of metagabbroic dykes in the peridotite. Although early metasomatism resulted in extensive rodingitization of the gabbros, some dykes show an eclogitic assemblage of Na-clinopyroxene + garnet + chloritoid + chlorite ± talc. These observations, the microstructures and the mineral chemistry all suggest that the assemblages in the ultramafic rocks and metagabbros developed during a prograde evolution towards high pressures (〉13–16 kbar, 450–550° C), and during subsequent decompression. This metamorphic evolution is considered to be related to Late Cretaceous intraoceanic subduction in the Alps-Apennine system and closure of the Piedmont-Ligurian basin.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1437-3262
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Abstract New data on major and trace elements geochemistry of the Assab Range (Ethiopia) basalts and enclosed mantle xenoliths are presented and discussed. Mantle ultramafics consist of spinel-peridotites and minor green spinel-pyroxenites (sometimes present as dykes within the former ones). Petrography and mineral chemistry indicate that both xenoliths families underwent a common subsolidus equilibrium crystallization at 1050°–1100° C., in the spinel-peridotite stability field. REE data on whole rock and on separated phases (cpx, opx and ol) have been obtained by RNAA. Spinel-peridotites exhibit LREE-enriched — HREE-depleted patterns with respect to chondrites. Mass balance calculations indicate that this is a characteristic feature of spinel-peridotite xenoliths which cannot be solely imputed to host basalt contamination. Xenoliths selected as representative of different depletion intensities, suffered by Assab spinel-peridotites prior to their subsolidus equilibration, show dependences from major elements composition in their REE geochemistry and wide variations in the measured REE partition values among coexisting phases. Concordancy in the REE compositions of liquids calculated utilizing the measured REE partitioning in the different xenoliths and theShaw's (1970) mass balance equation for non-modal equilibrium melting, confirms that the measured REE distribution represent equilibrium conditions. Theoretical least fusion liquids differ from the least differentiated among the enclosing basalts, both in their La/Lu ratio and in the total REE concentrations. Some similarities are observed with the composition of the pyroxenite dykes, however no firm conclusions on the comagmaticity of the two xenoliths types are reached. Trace geochemistry (REE, Ba, Sr, Cs, Rb, U, Th, Hf, Zr, Ta, Sc, Cr, Co, Ni: RNAA, INAA) on the host basalts indicates that the primary alkaline melts underwent an indipendent differentiation history by fractional crystallization at intermediate pressure conditions prior to the mantle xenoliths inclusion. Extrapolated seismic velocities for the Assab mantle xenoliths allow to ascribe them to the 7.3–7.7 VP layer, underlying the crustal layers in the Assab and Afar area, as recognized on the basis of the geophysical surveys. In light of the above evidences, an evolutive picture of the Assab association is proposed which takes into account present day knowledges on the geodynamic evolution of the Afar-Red Sea system.
    Abstract: Résumé Dans ce travail nous presentons des nouvelles données sur la géochimie des éléments majeurs et en traces dans les basaltes et dans les enclaves du manteau de la zone d'Assab (Éthiopie). Les enclaves; ultrabasiques du manteau sont constituées par des peridotites à spinelle et subordonnément par des pyroxenites à spinelle (quelquefois en forme de dykes dans les (peridotites). La pétrographie et la chimie des mineraux indiquent que les deux familles des enclaves esseurent une commune recristallization à l'équilibre aux temperatures de l'ordre de 1050°–1100° C dans le champ de stabilité de la peridotite à spinelle. Les données sur les terres rares dans la roche totale et dans les minéraux séparés ont été obtenues par RNAA. Les peridotites à spinelle montrent des patterns enrichis en terres rares légères et appauvries en terres rares lourdes par rapport à les aux condrites. Des calculs de balance de masse indiquent que cette caractéristique ne peut pas être attribuée simplément à la contamination par le basalte encaissant. Des enclaves sélectionées comme residus des differentes intensités de fusion partielle montrent des relations simples entre éléments majeurs et la géochimie des terres rares et des importantes variations des coefficients de partage des terres rares entre les differentes mineraux coexistants dans le même enclave. D'ailleurs la concordance entre les compositions en terres rares des differents liquides calculés à partir de la distribution des terres rares entre les mineraux des differents enclaves (en utilisant la loi deShaw, 1970) montre que les distributions mesurées sont representatives des conditions d'équilibre. Les liquides théoriques de fusion minime ont des valeurs differentes La/Lu et des teneurs differentes en terres rares par rapport à les laves aux encaissantes. Par contre quelque similitude peut-être envisagée avec les pyroxenites cependant les données actuelles ne permettent pas de rejoindre des conclusions sur la comagmaticitée des deux familles des enclaves. La géochimie des traces (REE, Ba, Sr, Cs, Rb, U, Th, Hf, Zr, Ta, Sc, Cr, Co, Ni: RNAA, INAA) sur les laves encaissantes montre que le magma alcalin primaire a differencié par cristallization fractionnée à des conditions de pression intermediaire avant d'encaisser les enclaves du manteau. Les vitesses seismiques déduites pour les enclaves du manteau à partir des données experimentales permettent d'identifier ces matériaux avec la couche à vitesse VP=7.3 –7.7 sous la région d'Assab et de l'Afar. Un modèle evolutif de l'association étudiée est presenté tout en considérant les conaissances actuelles de l'evolution geodinamique du sytème Afar-Mer Rouge.
    Notes: Zusammenfassung Die ultrabasischen Gesteine des Mantels der Zone Assab (Äthiopien) bestehen aus Spinell-Peridotiten und aus wenigen grünen Spinell-Pyroxeniten (manchmal sind sie in Form von Intrusivgängen in den Spinell-Peridotiten). Die Petrologie und die Mineralchemie zeigen, daß die zwei Xenolith-Familien eine gemeinsame Rekristallisation unter Gleichgewicht bei den Temperaturen 1050°–1100° C im Stabilitäts-Feld der Spinell-Peridotite hatten. Die Daten über die Seltenen Erden im Gesamtgestein und die getrennten Mineralien (cpx, opx und 01) wurden mit der RNAA-Methode erhalten. Die Spinell-Peridotite zeigen eine Anreicherung an leichten Seltenen Erden und eine Verarmung an schweren Seltenen Erden in Beziehung auf die Chondrite. Die Berechnungen der Massengleichgewichte zeigen an, daß dies eine Charakteristik von Spinell-Peridotit-Xenolithen darstellt, die nicht auf eine Verunreinigung durch die umgebenden Basalte zurückgeführt werden darf. Xenolithe aus verschiedenen Stadien der Aufschmelzung zeigen einfache Beziehungen zwischen Hauptelementen und der Geochemie der Seltenen Erden und weite Variationen der Verteilungs-Koeffizienten der Seltenen Erden unter koexistenten Phasen. Die Geochemie der Spurenelemente (REE, Ba, Sr, Cs, Rb, U, Th, Hf, Zr, Ta, Sc, Cr, Co, Ni: RNAA, INAA) in den Basalten zeigt, daß sich das primäre, alkalische Magma durch fraktionierte Kristallisation differenziert hat bevor die Peridotiteinschlüsse auftraten. Diese Beobachtungen stehen im Einklang mit der modernen Erkenntnis über die geodynamische Entwicklung der Afar-Region und des Roten Meeres.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 113 (1993), S. 437-449 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Ion probe investigations on mineral phases forming the Al-Di pyroxenites from the Zabargad peridotite body indicate that porphyroclastic pyroxenes in composite mafic layers record an unusual HREE, Zr, Sc enrichment not registered by pyroxenes in spinel websterites. Orthopyroxene in the opx+sp clusters forming the inner, cpx-free zone of layered pyroxenites shows strongly fractionated REE patterns (HREEN/LREEN〉1000; Yb〉100xch) and very high Zr, Sc and Y abundances (up to 30,672 and 60ppm, respectively). In the outer, cpx-rich zone porphyroclastic clinopyroxene is strongly HREE enriched (HREEN/LREEN∼29; Yb∼ 269xch) and displays very high Sc and Zr abundances (up to 819 and 164 ppm, respectively). It is suggested that the unusual trace element abundances are inherited from a precursor garnet. Composite pyroxenite layers are interpreted as former garnet clinopyroxenites characterized by gnt/cpx modal zoning. The sp+opx(cpx-free) assemblage in the inner part is a product of the break-down reaction of garnet upon decompression, with Ca of the original garnet completely entering the enstatite solid solution. The temperature at which the breakdown reaction occurred is estimated to be higher than 1000°C (P in the range 20–30 kbar). In the outer part, decompression caused the garnet to form a sp+opx assemblage; however, the grossularite component participated in the formation of new clinopyroxene which reacted with the clinopyroxene present in the original mode before the decompression reaction, thus forming a cpx2+sp+opx assemblage. As a result of garnet breakdown, pyroxenes have peculiar HFSE anomalies. Progressive upwelling during the Red Sea rifting produced incomplete reaction under pl-facies conditions. The geochemical signatures of precursor garnet in pyroxenes were partially crased during the recrystallization from granular spincl-bearing to granoblastic plagioclase-bearing assemblages, being preserved only in a few porphyroclast relies. The finding of pyroxenes with trace element characteristics of precursor garnet has important geodynamic and geochemical implications. Al-Di pyroxenite layers had a long history within the mantle, before the continental lithosphere rifting and thinning took place in the region. It is suggested that Al-Di pyroxenites were formed by deep-seated tholeiitic magmatism unrelated to the Red Sea evolution, thus representing the earliest event in the Zabargad upper mantle. Garnet breakdown significantly preceded the metasomatism induced by hydrous fluids (crystallization of Ti-rich pargasite) and the later intrusion of hydrous (Cr-Di) pyroxenite dykes. During the stages of mantle evolution, the HFSE anomalies in pyroxenes varied significantly. We note that the study of HFSE anomalies in mineral phases reveals complex geochemical histories which are not recorded by the whole-rock system.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract  Mantle peridotites of the Internal Liguride (IL) units (Northern Apennines) constitute a rare example of the depleted lithosphere of the Jurassic Ligurian Tethys. Detailed chemical (ICP-MS and SIMS techniques) and isotopic investigations on very fresh samples have been performed with the major aim to constrain the timing and mechanism of their evolution and to furnish new data for the geodynamic interpretation. The data are also useful to discuss some general geochemical aspects of oceanic-type mantle. The studied samples consist of clinopyroxene-poor spinel lherzolites, showing incipient re-equilibration in the plagioclase-facies stability field. The spinel-facies assemblage records high (asthenospheric) equilibration temperatures (1150–1250° C). Whole rocks, and constituent clinopyroxenes, show a decoupling between severe depletion in highly incompatible elements [light rare earth elements (LREE), Sr, Zr, Na, Ti] and less pronounced depletion in moderate incompatible elements (Ca, Al, Sc, V). Bulk rocks also display a relatively strong M(middle)REE/H(heavy)REE fractionation. These compositional features indicate low-degree (〈10%) fractional melting, which presumably started in the garnet stability field, as the most suitable depletion mechanism. In this respect, the IL ultramafics show strong similarity to abyssal peridotites. The Sr and Nd isotopic compositions, determined on carefully handpicked clinopyroxene separates, indicate an extremely depleted signature (87Sr/86Sr=0.702203–0.702285; 143Nd/144Nd=0.513619–0.513775). The Sm/Nd model ages suggest that the IL peridotites melted most likely during Permian times. They could record, therefore, the early upwelling and melting of mid ocean ridge basalt (MORB) type asthenosphere, in response to the onset of extensional mechanisms which led to the opening of the Western Tethys. They subsequently cooled and experienced a composite subsolidus evolution testified by multiple episodes of gabbroic intrusions and HT-LP retrograde metamorphic re-equilibration, prior to their emplacement on the sea floor. The trace element chemistry of IL peridotites also provides useful information about the composition of oceanic-type mantle. The most important feature concerns the occurrence of Sr and Zr negative anomalies (relative to “adjacent” REE) in both clinopyroxenes and bulk rocks. We suggest that such anomalies reflect changes in the relative magnitude of Sr, Zr and REE partition coefficients, depending on the specific melting conditions.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Mantle peridotites of the External Liguride (EL) Units (Northern Apennines) mainly consist of fertile spinel-lherzolites partially recrystallized to plagioclase-facies assemblages, and are consequently appropriate to investigate the interphase element partitioning related to the transition from spinel- to plagioclase-facies stability field. Evidence for the development of the plagioclase-facies assemblage is mainly given by: (1) large exsolution lamellae of orthopyroxene and plagioclase within spinel-facies clinopyroxene; (2) plagioclase rims around spinel; (3) granoblastic domains made up of olivine+plagioclase±clino-and orthopyroxene. In situ major and trace [REE (rare-earth elements), Ti, Sc, V, Cr, Sr, Y, Zr and Ba] element mineral analyses have been performed, by electron and ion probe, on selected samples which show the progressive development of the plagioclase-bearing assemblage. The main compositional variations observed during the change from spinel- to plagioclase-facies minerals are as follows: (1) clinopyroxenes decrease in Al, Na, Sr, Eu/Eu* and increase in Y, V, Sc, Cr, Zr and Ti; (2) amphiboles decrease in Eu/Eu*, Sr, Ba and increase in Zr and V; (3) spinels decrease in Al and increase in Cr and Ti. The most striking feature is the decoupling in the behaviour of similarly incompatible elements (D about 0.1) in clinopyroxene, e.g. Sr decrease is mirrored by Zr increase. Massbalance calculations indicate that the trace element interphase redistribution documented in the EL peridotites occurred in a closed system and in response to the metamorphic reaction governing the transition from the spinel- to the plagioclase-facies stability field. The observed element partitioning reveals, moreover, that subsolidus re-equilibration processes in the upper mantle produce HFSE (high-field-strength element)/REE fractionation in minerals, which must be evaluated for a reliable determination of mineral-melt distribution coefficients. The results of this study furnish evidence for subsolidus metamorphic evolution during decompression, without concomitant partial melting processes. This is consistent with the interpretation that the EL peridotites represent subcontinental lithospheric mantle emplaced at the surface in response to lithospheric thinning and tectonic denudation mechanisms related to the Triassic-Jurassic rifting of the Ligure-Piedmontese basin.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 83 (1983), S. 1-15 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Aluminous, magnesian metagabbroic layers and pods occur in the Beigua serpentinite of Western Liguria, where they are associated with more voluminous (Fe+Ti)-rich lithologies. Both types were subjected to localized early rodingitization. All rocks show the effects of a pervasive, essentially isochemical, high-pressure Early Alpine metamorphism for which a sequence of mineral assemblages is partially preserved: eclogite → glaucophanic eclogite → Na+Al actinolitic amphibolite → greenschist. The nature of the eo-Alpine high-pressure recrystallization, and the origin of the protoliths are the subjects of this paper. Eighteen new bulk rock XRF analyses for the magnesian metagabbros, combined with previously published major element analytical data for the ferroan metagabbros, demonstrate that a spectrum of compositions exist in the Gruppo di Voltri. This chemical range is comparable to differentiated oceanic tholeiites and to plutonic ophiolite suites cropping out elsewhere in the Northern Apennines and Western Alps. Both (Al+Mg)- and (Fe+Ti)-rich protoliths are regarded as the products of crystal fractionation of an original basaltic melt which intruded the Beigua mantle during the opening of Mesozoic Tethys. Textural observations show that local reactions along grain boundaries produced the garnet+sodic clinopyroxene assemblages from low-grade precursor phase compatibilities. Garnet coronas and zoned blue → blue-green → green amphiboles attest to the prevalence of domain equilibrium. Summarization of approximately 170 new mineral analyses documents this paragenesis. Assuming an attendant load pressure of about 10 Kb during formation of the eclogites, nominal temperatures of Fe-Mg partitioning between garnet and omphacite range from 483 to 544° C and average 508° C, in good agreement with petrologic constraints provided by the regional metamorphic assemblages in the enclosing antigoritic serpentinite and in adjacent parts of Western Liguria. The early stage of rodingitization and serpentinization is thought to reflect metasomatism and hydration in the vicinity of a Tethyan spreading center or fracture zone near the surface of the sea floor. In contrast, the subsequent high-pressure production of eclogites probably was a consequence of the profound subduction of oceanic crust and its mantle underpinnings during eo-Alpine convergence. Only the culmination of this prograde event has been preserved in the Gruppo di Voltri, but buoyant return towards upper crustal levels following decoupling is recorded in the eclogitized magnesian metagabbros by a decompression paragenetic series, successive stages of which are represented by glaucophanic eclogite, Na+Al actinolitic amphibolite and prasinite, respectively.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 115 (1993), S. 123-137 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Ion microprobe data (REE, Na, Sc, Ti, V, Cr, Sr, Zr) of unaltered clinopyroxenes in the ophiolitic basalts from the Northern Apennines have been used in a epx-based geochemical modelling of MORB magmatism from both External (EL) and Internal (IL) sectors of the Ligurian Tethys (i.e. Jurassic Ligure-Piemontese basin), alternative to the more common whole-rock approach. Clinopyroxenes from EL basalts display slightly fractionated LREE (CeN/SmN∼0.5) and HREE (GdN/ YbN∼1.5) patterns and large variations in the REE composition (up to 6 times from microphenocryst cores to interstitial clinopyroxenes). Interstitial clinopyroxenes in IL basalts are similar to the microphenocrysts from the most primitive EL basalts. By contrast, IL microphenocrysts are characterized by greater LREE (CeN/SmN ∼0.3) and lesser HREE (GdN/YbN〈1.2) fractionation. The comparison of trace element variations in wholerocks and clinopyroxenes clearly shows that the olivine and plagioclase portion of the fractionation sequence is poorly represented by the EL and IL basalts. In fact, ophiolitic basalts mainly consist of a minor interstitial glass (now deeply altered) associated with a prevailing plagioclase-clinopyroxene assemblage crystallized from liquids significantly evolved along the olivine-plagioclase-clinopyroxene saturation boundary. Thus, bulk rock chemistry is largely governed by clinopyroxene composition. This, in addition to alteration, indicates that the bulk rock chemistry does not provide reliable chemical information to constrain the composition and the generation of the parental magmas. Unfortunately, most clinopyroxenes are characterized by complex zoning, probably caused by disequilibrium partitioning during crystal growth as a result of kinetic factors. On this ground, estimation of melt chemistry and inferences about the origins of these basalts are only allowed by the core compositions of microphenocrystic clinopyroxenes. Modelling of (Nd/Yb)N and Ti/Zr in the parental magmas, as deduced from the clinopyroxene compositions, indicates thata EL and IL basalts do not represent products of different mantle source composition. Rather, they were generated by varying degrees of fractional melting in the spinel stability field, lower for the EL (a few percent) relative to IL, totalling no more than 10% of an asthenospheric MORB source, and leaving in the residua clinopyroxene with REE patterns similar to those shown by IL suboceanic type peridotites. Accordingly, these latter are interpreted as refractory residua after MORB-generating fractional melting occurred during rifting and opening of the Ligure-Piemontese basin. By contrast, residual clinopyroxenes from the EL subcontinental type peridotites are not consistent with low degrees of fractional melting in agreement with the current interpretation that EL peridotites are unrelated to the MORB magmatism in the Ligure-Piemontese basin and represent lithospheric mantle material already emplaced towards the surface by a tectonic denudation mechanism during the early stages of oceanic rifting.
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